Colon Cancer: Gene >> FAM98A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000238823
Start	33588342:33588342(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515A>G
AA Mutation	p.Glu172Gly(p.E172G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000238823
Start	33584945:33584945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755736838
CDS Mutation	c.1388G>A
AA Mutation	p.Gly463Glu(p.G463E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000238823
Start	33584946:33584946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1387G>A
AA Mutation	p.Gly463Arg(p.G463R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000238823
Start	33585180:33585180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1153G>T
AA Mutation	p.Asp385Tyr(p.D385Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000238823
Start	33585335:33585335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998C>G
AA Mutation	p.Thr333Arg(p.T333R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238823
Start	33585097:33585097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377624129
CDS Mutation	c.1236C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238823
Start	33584980:33584980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1353C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238823
Start	33585349:33585349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238823
Start	33588350:33588350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.507C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000238823
Start	33588335:33588335(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.522delA
AA Mutation	p.Lys174AsnfsTer2(p.K174Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000238823
Start	33584943:33584943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1390C>T
AA Mutation	p.Arg464Ter(p.R464*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FAM98A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000238823
Start	33585627:33585627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.791C>A
AA Mutation	p.Ser264Tyr(p.S264Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000238823
Start	33585593:33585593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.825G>A
Mutation Classification	Silent
Feature Type	Transcript